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Intestinal Lymphatic Transport of Halofantrine Occurs After Oral Administration of a Unit-Dose Lipid-Based Formulation to Fasted Dogs

โœ Scribed by Shui-Mei Khoo; David M. Shackleford; Christopher J. H. Porter; Glenn A. Edwards; William N. Charman


Book ID
111553147
Publisher
Springer US
Year
2003
Tongue
English
Weight
86 KB
Volume
20
Category
Article
ISSN
0724-8741

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A physicochemical basis for the extensiv
โœ Shui-Mei Khoo; Richard J. Prankerd; Glenn A. Edwards; Christopher J.H. Porter; W ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 180 KB

The highly lipid soluble, free-base form of halofantrine (Hf base; $ 50 mg/ mL in triglyceride lipids), a highly lipophilic (calculated log P $ 8.5) antimalarial, has recently been shown to undergo signiยฎcant intestinal lymphatic transport (54% of administered dose) after postprandial administration